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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7012836copy number variation1nstd229human GRCh38 chr19: 49,445,090-49,445,397 , GRCh37.p13 chr19: 49,948,347-49,948,654 PIH1D1
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6527046copy number variation1nstd223human GRCh38 chr19: 49,445,090-49,445,397 , GRCh37.p13 chr19: 49,948,347-49,948,654 PIH1D1
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6310544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758 CGB5, MED25, 76 more genes
    nsv6220648copy number variation1nstd214human GRCh38 chr19: 49,450,993-49,451,080 , GRCh37.p13 chr19: 49,954,250-49,954,337 PIH1D1
    nsv6146971copy number variation1nstd206human GRCh38 chr19: 49,446,874-49,481,000 , GRCh37.p13 chr19: 49,950,131-49,984,257 FLT3LG, PIH1D1, 1 more genes
    nsv6133706copy number variation1nstd213human GRCh37 chr19: 49,520,000-50,090,001 , GRCh38.p12 chr19: 49,016,743-49,586,744 CD37, CGB3, 51 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv6048537copy number variation1nstd212human GRCh38 chr19: 49,444,221-49,444,336 , GRCh37.p13 chr19: 49,947,478-49,947,593 PIH1D1
    nsv6041839copy number variation1nstd212human GRCh38 chr19: 49,448,983-49,449,056 , GRCh37.p13 chr19: 49,952,240-49,952,313 PIH1D1
    nsv5928362copy number variation1nstd209human GRCh38 chr19: 49,445,090-49,445,396 , GRCh37.p13 chr19: 49,948,347-49,948,653 PIH1D1
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5651357insertion1nstd207human GRCh38 chr19: 49,445,397-49,445,397 , GRCh37.p13 chr19: 49,948,654-49,948,654 PIH1D1
    nsv5528774copy number variation1nstd206human GRCh38 chr19: 49,445,090-49,445,397 , GRCh37.p13 chr19: 49,948,347-49,948,654 PIH1D1
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